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Thrombophilic gene polymorphism studies in G6PD deficient individuals from Saudi population
We performed a study to evaluate the role of three single nucleotide polymorphisms (SNPs), factor V Leiden G1691A (FVL), prothrombin gene mutation G20210A (PRT or FII-G20210A) and methylenotetrahydrofolate reductase variant C677T (MTHFRC677T), as risk factors for G6PD in Saudi populations. Our resul...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Biomedical Informatics
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3532010/ https://ncbi.nlm.nih.gov/pubmed/23275730 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6026/97320630081255 |
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